103206-21-9

Basic information

• Product Name: N,N-dimethyl-3-(phenylthio)aniline
• Synonyms: N,N-dimethyl-3-(phenylthio)aniline
• CAS NO: 103206-21-9
• Molecular Weight: 229.346
• Mol File: 103206-21-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N,N-dimethyl-3-(phenylthio)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethyl-3-(phenylthio)aniline(103206-21-9)
• EPA Substance Registry System: N,N-dimethyl-3-(phenylthio)aniline(103206-21-9)

Safety Data

• Hazardous Substances Data: 103206-21-9(Hazardous Substances Data)

Upstream product

• 3985-12-4 3-phenylthioaniline 
• 77-78-1 dimethyl sulfate 
• 16518-62-0 3-bromo-N,N-dimethylaniline 
• 178752-79-9 3-(N,N-dimethylamino)phenylboronic acid 
• 108-98-5 thiophenol 
• 6848-13-1 3-chloro-N,N-dimethylaniline 

Relevant articles and documents

Cross-Coupling of Chloro(hetero)arenes with Thiolates Employing a Ni(0)-Precatalyst

A general and efficient Ni-catalyzed coupling of challenging aryl chlorides and in situ generated aliphatic and aromatic thiolates is described. The employed on-cycle, air-stable defined Ni precatalysts allow for transformation of a broad scope of substrates. A variety of functional groups and heterocyclic motifs as well as structurally varied thiols are tolerated at unprecedented moderate catalyst loadings and reaction temperatures. Depending on reaction conditions, aryl thiols can selectively undergo C-S or C-C couplings.

Palladium-catalyzed carbon-sulfur cross-coupling reactions with indium tri(organothiolate) and its application to sequential one-pot processes

(Chemical Equation Presented) It was found that indium tri(organothiolate) is an effective nucleophilic coupling partner in Pd-catalyzed C-S cross-coupling reactions to produce the functionalized sulfides in excellent yields with high atom efficiency and